-
1
-
-
33745809841
-
Cystic fibrosis: terminology and diagnostic algorithms
-
2104676, 16384879
-
De Boeck K, Wilschanski M, Castellani C, Taylor C, Cuppens H, Dodge J, Sinaasappel M. Cystic fibrosis: terminology and diagnostic algorithms. Thorax 2006, 61(7):627-635. 10.1136/thx.2005.043539, 2104676, 16384879.
-
(2006)
Thorax
, vol.61
, Issue.7
, pp. 627-635
-
-
De Boeck, K.1
Wilschanski, M.2
Castellani, C.3
Taylor, C.4
Cuppens, H.5
Dodge, J.6
Sinaasappel, M.7
-
2
-
-
47049115524
-
Guidelines for diagnosis of cystic fibrosis in newborns through older adults: cystic fibrosis foundation consensus report
-
2810958, 18639722
-
Farrell PM, Rosenstein BJ, White TB, Accurso FJ, Castellani C, Cutting GR, Durie PR, Legrys VA, Massie J, Parad RB, Rock MJ, Campbell PW. Guidelines for diagnosis of cystic fibrosis in newborns through older adults: cystic fibrosis foundation consensus report. J Pediatr 2008, 153(2):S4-S14. 10.1016/j.jpeds.2008.05.005, 2810958, 18639722.
-
(2008)
J Pediatr
, vol.153
, Issue.2
, pp. S4-S14
-
-
Farrell, P.M.1
Rosenstein, B.J.2
White, T.B.3
Accurso, F.J.4
Castellani, C.5
Cutting, G.R.6
Durie, P.R.7
Legrys, V.A.8
Massie, J.9
Parad, R.B.10
Rock, M.J.11
Campbell, P.W.12
-
3
-
-
84862770787
-
Role of cystic fibrosis transmembrane conductance regulator in patients with chronic sinopulmonary disease
-
22423042
-
Gonska T, Choi P, Stephenson A, Ellis L, Martin S, Solomon M, Dupuis A, Dorfman R, Zielenski J, Ooi CY, Weiser W, Durie PR, Tullis E. Role of cystic fibrosis transmembrane conductance regulator in patients with chronic sinopulmonary disease. Chest 2012, 142(4):996-1004. 10.1378/chest.11-2543, 22423042.
-
(2012)
Chest
, vol.142
, Issue.4
, pp. 996-1004
-
-
Gonska, T.1
Choi, P.2
Stephenson, A.3
Ellis, L.4
Martin, S.5
Solomon, M.6
Dupuis, A.7
Dorfman, R.8
Zielenski, J.9
Ooi, C.Y.10
Weiser, W.11
Durie, P.R.12
Tullis, E.13
-
4
-
-
84893972760
-
Does extensive genotyping and nasal potential difference testing clarify the diagnosis of cystic fibrosis among patients with single-organ manifestations of cystic fibrosis?
-
24149827
-
Ooi CY, Dupuis A, Ellis L, Jarvi K, Martin S, Ray PN, Steele L, Kortan P, Gonska T, Dorfman R, Solomon M, Zielenski J, Corey M, Tullis E, Durie P. Does extensive genotyping and nasal potential difference testing clarify the diagnosis of cystic fibrosis among patients with single-organ manifestations of cystic fibrosis?. Thorax 2014, 69(3):254-260. 10.1136/thoraxjnl-2013-203832, 24149827.
-
(2014)
Thorax
, vol.69
, Issue.3
, pp. 254-260
-
-
Ooi, C.Y.1
Dupuis, A.2
Ellis, L.3
Jarvi, K.4
Martin, S.5
Ray, P.N.6
Steele, L.7
Kortan, P.8
Gonska, T.9
Dorfman, R.10
Solomon, M.11
Zielenski, J.12
Corey, M.13
Tullis, E.14
Durie, P.15
-
5
-
-
53749101293
-
Cystic fibrosis transmembrane conductance regulator ion channel function testing in recurrent acute pancreatitis
-
18360295
-
Segal I, Yaakov Y, Adler SN, Blau H, Broide E, Santo M, Yahav Y, Klar A, Lerner A, Aviram M, Ellis I, Mountford R, Shteyer E, Kerem E, Wilschanski M. Cystic fibrosis transmembrane conductance regulator ion channel function testing in recurrent acute pancreatitis. J Clin Gastroenterol 2008, 42(7):810-814. 10.1097/MCG.0b013e318156617c, 18360295.
-
(2008)
J Clin Gastroenterol
, vol.42
, Issue.7
, pp. 810-814
-
-
Segal, I.1
Yaakov, Y.2
Adler, S.N.3
Blau, H.4
Broide, E.5
Santo, M.6
Yahav, Y.7
Klar, A.8
Lerner, A.9
Aviram, M.10
Ellis, I.11
Mountford, R.12
Shteyer, E.13
Kerem, E.14
Wilschanski, M.15
-
6
-
-
84862763252
-
Comparing the American and European diagnostic guidelines for cystic fibrosis: same disease, different language?
-
22504961
-
Ooi CY, Dupuis A, Ellis L, Jarvi K, Martin S, Gonska T, Dorfman R, Kortan P, Solomon M, Tullis E, Durie PR. Comparing the American and European diagnostic guidelines for cystic fibrosis: same disease, different language?. Thorax 2012, 67(7):618-624. 10.1136/thoraxjnl-2011-201454, 22504961.
-
(2012)
Thorax
, vol.67
, Issue.7
, pp. 618-624
-
-
Ooi, C.Y.1
Dupuis, A.2
Ellis, L.3
Jarvi, K.4
Martin, S.5
Gonska, T.6
Dorfman, R.7
Kortan, P.8
Solomon, M.9
Tullis, E.10
Durie, P.R.11
-
7
-
-
84872190665
-
CFTR biomarkers: time for promotion to surrogate end-point
-
22878883
-
De Boeck K, Kent L, Davies J, Derichs N, Amaral M, Rowe SM, Middleton P, de Jonge H, Bronsveld I, Wilschanski M, Melotti P, Danner-Boucher I, Boerner S, Fajac I, Southern K, de Nooijer RA, Bot A, de Rijke Y, de Wachter E, Leal T, Vermeulen F, Hug MJ, Rault G, Nguyen-Khoa T, Barreto C, Proesmans M, Sermet-Gaudelus I. CFTR biomarkers: time for promotion to surrogate end-point. Eur Respir J 2013, 41(1):203-216. 10.1183/09031936.00057512, 22878883.
-
(2013)
Eur Respir J
, vol.41
, Issue.1
, pp. 203-216
-
-
De Boeck, K.1
Kent, L.2
Davies, J.3
Derichs, N.4
Amaral, M.5
Rowe, S.M.6
Middleton, P.7
de Jonge, H.8
Bronsveld, I.9
Wilschanski, M.10
Melotti, P.11
Danner-Boucher, I.12
Boerner, S.13
Fajac, I.14
Southern, K.15
de Nooijer, R.A.16
Bot, A.17
de Rijke, Y.18
de Wachter, E.19
Leal, T.20
Vermeulen, F.21
Hug, M.J.22
Rault, G.23
Nguyen-Khoa, T.24
Barreto, C.25
Proesmans, M.26
Sermet-Gaudelus, I.27
more..
-
8
-
-
80052340084
-
Nasal potential difference measurements to assess CFTR ion channel activity
-
3760477, 21594779
-
Rowe SM, Clancy JP, Wilschanski M. Nasal potential difference measurements to assess CFTR ion channel activity. Methods Mol Biol 2011, 741:69-86. 10.1007/978-1-61779-117-8_6, 3760477, 21594779.
-
(2011)
Methods Mol Biol
, vol.741
, pp. 69-86
-
-
Rowe, S.M.1
Clancy, J.P.2
Wilschanski, M.3
-
9
-
-
80052320123
-
Measurement of ion transport function in rectal biopsies
-
21594780
-
Hug MJ, Derichs N, Bronsveld I, Clancy JP. Measurement of ion transport function in rectal biopsies. Methods Mol Biol 2011, 741:87-107. 10.1007/978-1-61779-117-8_7, 21594780.
-
(2011)
Methods Mol Biol
, vol.741
, pp. 87-107
-
-
Hug, M.J.1
Derichs, N.2
Bronsveld, I.3
Clancy, J.P.4
-
10
-
-
85010429275
-
Multicenter European Standardization and reference values for intestinal current measurement in rectal biopsies
-
Derichs N, Pinders-Kessler L, Bronsveld I, Scheinert S, Rückes-Nilges C, de Jonge H, Nährlich L. Multicenter European Standardization and reference values for intestinal current measurement in rectal biopsies. Pediatr Pulmonol 2013, 48(S36):300.
-
(2013)
Pediatr Pulmonol
, vol.48
, Issue.S36
, pp. 300
-
-
Derichs, N.1
Pinders-Kessler, L.2
Bronsveld, I.3
Scheinert, S.4
Rückes-Nilges, C.5
de Jonge, H.6
Nährlich, L.7
-
11
-
-
84867641604
-
Measurements of CFTR-mediated Cl- secretion in human rectal biopsies constitute a robust biomarker for Cystic Fibrosis diagnosis and prognosis
-
3474728, 23082198
-
Sousa M, Servidoni MF, Vinagre AM, Ramalho AS, Bonadia LC, Felicio V, Ribeiro MA, Uliyakina I, Marson FA, Kmit A, Cardoso SR, Ribeiro JD, Bertuzzo CS, Sousa L, Kunzelmann K, Ribeiro AF, Amaral MD. Measurements of CFTR-mediated Cl- secretion in human rectal biopsies constitute a robust biomarker for Cystic Fibrosis diagnosis and prognosis. PLoS One 2012, 7(10):e47708. 10.1371/journal.pone.0047708, 3474728, 23082198.
-
(2012)
PLoS One
, vol.7
, Issue.10
, pp. e47708
-
-
Sousa, M.1
Servidoni, M.F.2
Vinagre, A.M.3
Ramalho, A.S.4
Bonadia, L.C.5
Felicio, V.6
Ribeiro, M.A.7
Uliyakina, I.8
Marson, F.A.9
Kmit, A.10
Cardoso, S.R.11
Ribeiro, J.D.12
Bertuzzo, C.S.13
Sousa, L.14
Kunzelmann, K.15
Ribeiro, A.F.16
Amaral, M.D.17
-
12
-
-
77955298789
-
Intestinal current measurement for diagnostic classification of patients with questionable cystic fibrosis: validation and reference data
-
20627915
-
Derichs N, Sanz J, Von Kanel T, Stolpe C, Zapf A, Tummler B, Gallati S, Ballmann M. Intestinal current measurement for diagnostic classification of patients with questionable cystic fibrosis: validation and reference data. Thorax 2010, 65(7):594-599. 10.1136/thx.2009.125088, 20627915.
-
(2010)
Thorax
, vol.65
, Issue.7
, pp. 594-599
-
-
Derichs, N.1
Sanz, J.2
Von Kanel, T.3
Stolpe, C.4
Zapf, A.5
Tummler, B.6
Gallati, S.7
Ballmann, M.8
-
13
-
-
84890439076
-
J. B., Solomon MG, Calancy JP, Rowe SM: Normative values and receiver operating characteristics of NPD for diagnostic measurements
-
Liu B, Hathorne H, Hill A, Cohen M. J. B., Solomon MG, Calancy JP, Rowe SM: Normative values and receiver operating characteristics of NPD for diagnostic measurements. Pediatr Pulmonol 2010, 303(S33):307.
-
(2010)
Pediatr Pulmonol
, vol.303
, Issue.S33
, pp. 307
-
-
Liu, B.1
Hathorne, H.2
Hill, A.3
Cohen, M.4
-
14
-
-
0028991826
-
In vivo nasal potential difference: techniques and protocols for assessing efficacy of gene transfer in cystic fibrosis
-
7542031
-
Knowles MR, Paradiso AM, Boucher RC. In vivo nasal potential difference: techniques and protocols for assessing efficacy of gene transfer in cystic fibrosis. Hum Gene Ther 1995, 6(4):445-455. 10.1089/hum.1995.6.4-445, 7542031.
-
(1995)
Hum Gene Ther
, vol.6
, Issue.4
, pp. 445-455
-
-
Knowles, M.R.1
Paradiso, A.M.2
Boucher, R.C.3
-
15
-
-
5144232620
-
CFTR Cl- channel function in native human colon correlates with the genotype and phenotype in cystic fibrosis
-
15480987
-
Hirtz S, Gonska T, Seydewitz HH, Thomas J, Greiner P, Kuehr J, Brandis M, Eichler I, Rocha H, Lopes AI, Barreto C, Ramalho A, Amaral MD, Kunzelmann K, Mall M. CFTR Cl- channel function in native human colon correlates with the genotype and phenotype in cystic fibrosis. Gastroenterology 2004, 127(4):1085-1095. 10.1053/j.gastro.2004.07.006, 15480987.
-
(2004)
Gastroenterology
, vol.127
, Issue.4
, pp. 1085-1095
-
-
Hirtz, S.1
Gonska, T.2
Seydewitz, H.H.3
Thomas, J.4
Greiner, P.5
Kuehr, J.6
Brandis, M.7
Eichler, I.8
Rocha, H.9
Lopes, A.I.10
Barreto, C.11
Ramalho, A.12
Amaral, M.D.13
Kunzelmann, K.14
Mall, M.15
-
16
-
-
84874117123
-
Evaluation of the intestinal current measurement method as a diagnostic test for cystic fibrosis
-
22553157
-
Cohen-Cymberknoh M, Yaakov Y, Shoseyov D, Shteyer E, Schachar E, Rivlin J, Bentur L, Picard E, Aviram M, Israeli E, Kerem E, Wilschanski M. Evaluation of the intestinal current measurement method as a diagnostic test for cystic fibrosis. Pediatr Pulmonol 2013, 48(3):229-235. 10.1002/ppul.22586, 22553157.
-
(2013)
Pediatr Pulmonol
, vol.48
, Issue.3
, pp. 229-235
-
-
Cohen-Cymberknoh, M.1
Yaakov, Y.2
Shoseyov, D.3
Shteyer, E.4
Schachar, E.5
Rivlin, J.6
Bentur, L.7
Picard, E.8
Aviram, M.9
Israeli, E.10
Kerem, E.11
Wilschanski, M.12
-
17
-
-
33646540731
-
Cystic fibrosis transmembrane conductance regulator function is suppressed in cigarette smokers
-
16497995
-
Cantin AM, Hanrahan JW, Bilodeau G, Ellis L, Dupuis A, Liao J, Zielenski J, Durie P. Cystic fibrosis transmembrane conductance regulator function is suppressed in cigarette smokers. Am J Respir Crit Care Med 2006, 173(10):1139-1144. 10.1164/rccm.200508-1330OC, 16497995.
-
(2006)
Am J Respir Crit Care Med
, vol.173
, Issue.10
, pp. 1139-1144
-
-
Cantin, A.M.1
Hanrahan, J.W.2
Bilodeau, G.3
Ellis, L.4
Dupuis, A.5
Liao, J.6
Zielenski, J.7
Durie, P.8
-
18
-
-
84890050882
-
Cigarette smoke induces systemic defects in cystic fibrosis transmembrane conductance regulator function
-
24040746
-
Raju SV, Jackson PL, Courville CA, McNicholas CM, Sloane PA, Sabbatini G, Tidwell S, Tang LP, Liu B, Fortenberry JA, Jones CW, Boydston JA, Clancy JP, Bowen LE, Accurso FJ, Blalock JE, Dransfield MT, Rowe SM. Cigarette smoke induces systemic defects in cystic fibrosis transmembrane conductance regulator function. Am J Respir Crit Care Med 2013, 188(11):1321-1330. 10.1164/rccm.201304-0733OC, 24040746.
-
(2013)
Am J Respir Crit Care Med
, vol.188
, Issue.11
, pp. 1321-1330
-
-
Raju, S.V.1
Jackson, P.L.2
Courville, C.A.3
McNicholas, C.M.4
Sloane, P.A.5
Sabbatini, G.6
Tidwell, S.7
Tang, L.P.8
Liu, B.9
Fortenberry, J.A.10
Jones, C.W.11
Boydston, J.A.12
Clancy, J.P.13
Bowen, L.E.14
Accurso, F.J.15
Blalock, J.E.16
Dransfield, M.T.17
Rowe, S.M.18
-
20
-
-
17844376483
-
Nasal potential difference measurements in patients with atypical cystic fibrosis
-
11491166
-
Wilschanski M, Famini H, Strauss-Liviatan N, Rivlin J, Blau H, Bibi H, Bentur L, Yahav Y, Springer H, Kramer MR, Klar A, Ilani A, Kerem B, Kerem E. Nasal potential difference measurements in patients with atypical cystic fibrosis. Eur Respir J 2001, 17(6):1208-1215. 10.1183/09031936.01.00092501, 11491166.
-
(2001)
Eur Respir J
, vol.17
, Issue.6
, pp. 1208-1215
-
-
Wilschanski, M.1
Famini, H.2
Strauss-Liviatan, N.3
Rivlin, J.4
Blau, H.5
Bibi, H.6
Bentur, L.7
Yahav, Y.8
Springer, H.9
Kramer, M.R.10
Klar, A.11
Ilani, A.12
Kerem, B.13
Kerem, E.14
-
21
-
-
0025609981
-
Nasal potential difference: a clinical diagnostic test for cystic fibrosis
-
Alton EW, Currie D, Logan-Sinclair R, Warner JO, Hodson ME, Geddes DM. Nasal potential difference: a clinical diagnostic test for cystic fibrosis. Eur Respir J 1990, 3(8):922-926.
-
(1990)
Eur Respir J
, vol.3
, Issue.8
, pp. 922-926
-
-
Alton, E.W.1
Currie, D.2
Logan-Sinclair, R.3
Warner, J.O.4
Hodson, M.E.5
Geddes, D.M.6
-
22
-
-
0023641255
-
Clinical application of transepithelial potential difference measurements in cystic fibrosis
-
2442338
-
Sauder RA, Chesrown SE, Loughlin GM. Clinical application of transepithelial potential difference measurements in cystic fibrosis. J Pediatr 1987, 111(3):353-358. 10.1016/S0022-3476(87)80453-5, 2442338.
-
(1987)
J Pediatr
, vol.111
, Issue.3
, pp. 353-358
-
-
Sauder, R.A.1
Chesrown, S.E.2
Loughlin, G.M.3
-
23
-
-
77956103863
-
Measurement of airway ion transport assists the diagnosis of cystic fibrosis
-
20597077
-
Middleton PG, House HH. Measurement of airway ion transport assists the diagnosis of cystic fibrosis. Pediatr Pulmonol 2010, 45(8):789-795. 10.1002/ppul.21253, 20597077.
-
(2010)
Pediatr Pulmonol
, vol.45
, Issue.8
, pp. 789-795
-
-
Middleton, P.G.1
House, H.H.2
-
24
-
-
33749446633
-
Mutations in the cystic fibrosis transmembrane regulator gene and in vivo transepithelial potentials
-
2648063, 16840743
-
Wilschanski M, Dupuis A, Ellis L, Jarvi K, Zielenski J, Tullis E, Martin S, Corey M, Tsui LC, Durie P. Mutations in the cystic fibrosis transmembrane regulator gene and in vivo transepithelial potentials. Am J Respir Crit Care Med 2006, 174(7):787-794. 10.1164/rccm.200509-1377OC, 2648063, 16840743.
-
(2006)
Am J Respir Crit Care Med
, vol.174
, Issue.7
, pp. 787-794
-
-
Wilschanski, M.1
Dupuis, A.2
Ellis, L.3
Jarvi, K.4
Zielenski, J.5
Tullis, E.6
Martin, S.7
Corey, M.8
Tsui, L.C.9
Durie, P.10
-
25
-
-
0030960151
-
Relationship between airway ion transport and a mild pulmonary disease mutation in CFTR
-
9154877
-
Walker LC, Venglarik CJ, Aubin G, Weatherly MR, McCarty NA, Lesnick B, Ruiz F, Clancy JP, Sorscher EJ. Relationship between airway ion transport and a mild pulmonary disease mutation in CFTR. Am J Respir Crit Care Med 1997, 155(5):1684-1689. 10.1164/ajrccm.155.5.9154877, 9154877.
-
(1997)
Am J Respir Crit Care Med
, vol.155
, Issue.5
, pp. 1684-1689
-
-
Walker, L.C.1
Venglarik, C.J.2
Aubin, G.3
Weatherly, M.R.4
McCarty, N.A.5
Lesnick, B.6
Ruiz, F.7
Clancy, J.P.8
Sorscher, E.J.9
-
26
-
-
0035213684
-
Chloride conductance and genetic background modulate the cystic fibrosis phenotype of Delta F508 homozygous twins and siblings
-
200980, 11733566
-
Bronsveld I, Mekus F, Bijman J, Ballmann M, de Jonge HR, Laabs U, Halley DJ, Ellemunter H, Mastella G, Thomas S, Veeze HJ, Tummler B. Chloride conductance and genetic background modulate the cystic fibrosis phenotype of Delta F508 homozygous twins and siblings. J Clin Invest 2001, 108(11):1705-1715. 10.1172/JCI12108, 200980, 11733566.
-
(2001)
J Clin Invest
, vol.108
, Issue.11
, pp. 1705-1715
-
-
Bronsveld, I.1
Mekus, F.2
Bijman, J.3
Ballmann, M.4
de Jonge, H.R.5
Laabs, U.6
Halley, D.J.7
Ellemunter, H.8
Mastella, G.9
Thomas, S.10
Veeze, H.J.11
Tummler, B.12
-
27
-
-
44949157170
-
Airway ion transport impacts on disease presentation and severity in cystic fibrosis
-
Leal T, Fajac I, Wallace HL, Lebecque P, Lebacq J, Hubert D, Dall'Ava J, Dusser D, Ganesan AP, Knoop C, Cumps J, Wallemacq P, Southern KW. Airway ion transport impacts on disease presentation and severity in cystic fibrosis. Clin Biochem 2008, 41(10-11):764-772.
-
(2008)
Clin Biochem
, vol.41
, Issue.10-11
, pp. 764-772
-
-
Leal, T.1
Fajac, I.2
Wallace, H.L.3
Lebecque, P.4
Lebacq, J.5
Hubert, D.6
Dall'Ava, J.7
Dusser, D.8
Ganesan, A.P.9
Knoop, C.10
Cumps, J.11
Wallemacq, P.12
Southern, K.W.13
-
28
-
-
0042877070
-
Nasal airway ion transport and lung function in young people with cystic fibrosis
-
12829453
-
Wallace HL, Barker PM, Southern KW. Nasal airway ion transport and lung function in young people with cystic fibrosis. Am J Respir Crit Care Med 2003, 168(5):594-600. 10.1164/rccm.200211-1302OC, 12829453.
-
(2003)
Am J Respir Crit Care Med
, vol.168
, Issue.5
, pp. 594-600
-
-
Wallace, H.L.1
Barker, P.M.2
Southern, K.W.3
-
29
-
-
84890429584
-
Nasal potential difference measurements in diagnosis of cystic fibrosis: An international survey
-
24022019
-
Naehrlich L, Ballmann M, Davies J, Derichs N, Gonska T, Hjelte L, van Konigsbruggen-Rietschel S, Leal T, Melotti P, Middleton P, Tummler B, Vermeulen F, Wilschanski M. Nasal potential difference measurements in diagnosis of cystic fibrosis: An international survey. J Cyst Fibros 2014, 13(1):24-28. 10.1016/j.jcf.2013.08.006, 24022019.
-
(2014)
J Cyst Fibros
, vol.13
, Issue.1
, pp. 24-28
-
-
Naehrlich, L.1
Ballmann, M.2
Davies, J.3
Derichs, N.4
Gonska, T.5
Hjelte, L.6
van Konigsbruggen-Rietschel, S.7
Leal, T.8
Melotti, P.9
Middleton, P.10
Tummler, B.11
Vermeulen, F.12
Wilschanski, M.13
-
30
-
-
77958180032
-
Clinical phenotype and genotype of children with borderline sweat test and abnormal nasal epithelial chloride transport
-
20538955
-
Sermet-Gaudelus I, Girodon E, Sands D, Stremmler N, Vavrova V, Deneuville E, Reix P, Bui S, Huet F, Lebourgeois M, Munck A, Iron A, Skalicka V, Bienvenu T, Roussel D, Lenoir G, Bellon G, Sarles J, Macek M, Roussey M, Fajac I, Edelman A. Clinical phenotype and genotype of children with borderline sweat test and abnormal nasal epithelial chloride transport. Am J Respir Crit Care Med 2010, 182(7):929-936. 10.1164/rccm.201003-0382OC, 20538955.
-
(2010)
Am J Respir Crit Care Med
, vol.182
, Issue.7
, pp. 929-936
-
-
Sermet-Gaudelus, I.1
Girodon, E.2
Sands, D.3
Stremmler, N.4
Vavrova, V.5
Deneuville, E.6
Reix, P.7
Bui, S.8
Huet, F.9
Lebourgeois, M.10
Munck, A.11
Iron, A.12
Skalicka, V.13
Bienvenu, T.14
Roussel, D.15
Lenoir, G.16
Bellon, G.17
Sarles, J.18
Macek, M.19
Roussey, M.20
Fajac, I.21
Edelman, A.22
more..
-
31
-
-
0028218460
-
Determinants of mild clinical symptoms in cystic fibrosis patients. Residual chloride secretion measured in rectal biopsies in relation to the genotype
-
293855, 8113384
-
Veeze HJ, Halley DJ, Bijman J, de Jongste JC, de Jonge HR, Sinaasappel M. Determinants of mild clinical symptoms in cystic fibrosis patients. Residual chloride secretion measured in rectal biopsies in relation to the genotype. J Clin Invest 1994, 93(2):461-466. 10.1172/JCI116993, 293855, 8113384.
-
(1994)
J Clin Invest
, vol.93
, Issue.2
, pp. 461-466
-
-
Veeze, H.J.1
Halley, D.J.2
Bijman, J.3
de Jongste, J.C.4
de Jonge, H.R.5
Sinaasappel, M.6
-
32
-
-
11044232030
-
Ex vivo CF diagnosis by intestinal current measurements (ICM) in small aperture, circulating Ussing chambers
-
De Jonge HR, Ballmann M, Veeze H, Bronsveld I, Stanke F, Tummler B, Sinaasappel M. Ex vivo CF diagnosis by intestinal current measurements (ICM) in small aperture, circulating Ussing chambers. J Cyst Fibros 2004, 3(Suppl 2):159-163.
-
(2004)
J Cyst Fibros
, vol.3
, Issue.SUPPL 2
, pp. 159-163
-
-
De Jonge, H.R.1
Ballmann, M.2
Veeze, H.3
Bronsveld, I.4
Stanke, F.5
Tummler, B.6
Sinaasappel, M.7
-
33
-
-
0025772974
-
Ion transport abnormalities in rectal suction biopsies from children with cystic fibrosis
-
Veeze HJ, Sinaasappel M, Bijman J, Bouquet J, de Jonge HR. Ion transport abnormalities in rectal suction biopsies from children with cystic fibrosis. Gastroenterology 1991, 101(2):398-403.
-
(1991)
Gastroenterology
, vol.101
, Issue.2
, pp. 398-403
-
-
Veeze, H.J.1
Sinaasappel, M.2
Bijman, J.3
Bouquet, J.4
de Jonge, H.R.5
-
34
-
-
84883799745
-
Multicenter intestinal current measurements in rectal biopsies from CF and non-CF subjects to monitor CFTR function
-
3769519, 24040112
-
Clancy JP, Szczesniak RD, Ashlock MA, Ernst SE, Fan L, Hornick DB, Karp PH, Khan U, Lymp J, Ostmann AJ, Rezayat A, Starner TD, Sugandha SP, Sun H, Quinney N, Donaldson SH, Rowe SM, Gabriel SE. Multicenter intestinal current measurements in rectal biopsies from CF and non-CF subjects to monitor CFTR function. PLoS One 2013, 8(9):e73905. 10.1371/journal.pone.0073905, 3769519, 24040112.
-
(2013)
PLoS One
, vol.8
, Issue.9
, pp. e73905
-
-
Clancy, J.P.1
Szczesniak, R.D.2
Ashlock, M.A.3
Ernst, S.E.4
Fan, L.5
Hornick, D.B.6
Karp, P.H.7
Khan, U.8
Lymp, J.9
Ostmann, A.J.10
Rezayat, A.11
Starner, T.D.12
Sugandha, S.P.13
Sun, H.14
Quinney, N.15
Donaldson, S.H.16
Rowe, S.M.17
Gabriel, S.E.18
-
35
-
-
0033646566
-
Active intestinal chloride secretion in human carriers of cystic fibrosis mutations: an evaluation of the hypothesis that heterozygotes have subnormal active intestinal chloride secretion
-
1287919, 11055897
-
Hogenauer C, Santa Ana CA, Porter JL, Millard M, Gelfand A, Rosenblatt RL, Prestidge CB, Fordtran JS. Active intestinal chloride secretion in human carriers of cystic fibrosis mutations: an evaluation of the hypothesis that heterozygotes have subnormal active intestinal chloride secretion. Am J Hum Genet 2000, 67(6):1422-1427. 10.1086/316911, 1287919, 11055897.
-
(2000)
Am J Hum Genet
, vol.67
, Issue.6
, pp. 1422-1427
-
-
Hogenauer, C.1
Santa Ana, C.A.2
Porter, J.L.3
Millard, M.4
Gelfand, A.5
Rosenblatt, R.L.6
Prestidge, C.B.7
Fordtran, J.S.8
-
36
-
-
0032588980
-
DeltaF508 CFTR protein expression in tissues from patients with cystic fibrosis
-
408454, 10330420
-
Kalin N, Claass A, Sommer M, Puchelle E, Tummler B. DeltaF508 CFTR protein expression in tissues from patients with cystic fibrosis. J Clin Invest 1999, 103(10):1379-1389. 10.1172/JCI5731, 408454, 10330420.
-
(1999)
J Clin Invest
, vol.103
, Issue.10
, pp. 1379-1389
-
-
Kalin, N.1
Claass, A.2
Sommer, M.3
Puchelle, E.4
Tummler, B.5
-
37
-
-
84874614232
-
Apical CFTR expression in human nasal epithelium correlates with lung disease in cystic fibrosis
-
3590182, 23483918
-
van Meegen MA, Terheggen-Lagro SW, Koymans KJ, van der Ent CK, Beekman JM. Apical CFTR expression in human nasal epithelium correlates with lung disease in cystic fibrosis. PLoS One 2013, 8(3):e57617. 10.1371/journal.pone.0057617, 3590182, 23483918.
-
(2013)
PLoS One
, vol.8
, Issue.3
, pp. e57617
-
-
van Meegen, M.A.1
Terheggen-Lagro, S.W.2
Koymans, K.J.3
van der Ent, C.K.4
Beekman, J.M.5
-
38
-
-
77956649717
-
Functional analysis of F508del CFTR in native human colon
-
20696241
-
van Barneveld A, Stanke F, Tamm S, Siebert B, Brandes G, Derichs N, Ballmann M, Junge S, Tummler B. Functional analysis of F508del CFTR in native human colon. Biochim Biophys Acta 2010, 1802(11):1062-1069. 10.1016/j.bbadis.2010.08.001, 20696241.
-
(2010)
Biochim Biophys Acta
, vol.1802
, Issue.11
, pp. 1062-1069
-
-
van Barneveld, A.1
Stanke, F.2
Tamm, S.3
Siebert, B.4
Brandes, G.5
Derichs, N.6
Ballmann, M.7
Junge, S.8
Tummler, B.9
-
39
-
-
0033865589
-
Role of CFTR in the colon
-
10845099
-
Greger R. Role of CFTR in the colon. Annu Rev Physiol 2000, 62:467-491. 10.1146/annurev.physiol.62.1.467, 10845099.
-
(2000)
Annu Rev Physiol
, vol.62
, pp. 467-491
-
-
Greger, R.1
-
40
-
-
0035694436
-
The effects of coronavirus on human nasal ciliated respiratory epithelium
-
11829103
-
Chilvers MA, McKean M, Rutman A, Myint BS, Silverman M, O'Callaghan C. The effects of coronavirus on human nasal ciliated respiratory epithelium. Eur Respir J 2001, 18(6):965-970. 10.1183/09031936.01.00093001, 11829103.
-
(2001)
Eur Respir J
, vol.18
, Issue.6
, pp. 965-970
-
-
Chilvers, M.A.1
McKean, M.2
Rutman, A.3
Myint, B.S.4
Silverman, M.5
O'Callaghan, C.6
-
41
-
-
76249104369
-
Rhinovirus infection-induced alteration of tight junction and adherens junction components in human nasal epithelial cells
-
Yeo NK, Jang YJ. Rhinovirus infection-induced alteration of tight junction and adherens junction components in human nasal epithelial cells. Laryngoscope 2010, 120(2):346-352.
-
(2010)
Laryngoscope
, vol.120
, Issue.2
, pp. 346-352
-
-
Yeo, N.K.1
Jang, Y.J.2
-
42
-
-
0028947884
-
Decreased expression of the CFTR protein in remodeled human nasal epithelium from non-cystic fibrosis patients
-
Brezillon S, Dupuit F, Hinnrasky J, Marchand V, Kalin N, Tummler B, Puchelle E. Decreased expression of the CFTR protein in remodeled human nasal epithelium from non-cystic fibrosis patients. Lab Invest 1995, 72(2):191-200.
-
(1995)
Lab Invest
, vol.72
, Issue.2
, pp. 191-200
-
-
Brezillon, S.1
Dupuit, F.2
Hinnrasky, J.3
Marchand, V.4
Kalin, N.5
Tummler, B.6
Puchelle, E.7
-
43
-
-
0021352368
-
Bioelectric properties and ion flow across excised human bronchi
-
Knowles M, Murray G, Shallal J, Askin F, Ranga V, Gatzy J, Boucher R. Bioelectric properties and ion flow across excised human bronchi. J Appl Physiol 1984, 56(4):868-877.
-
(1984)
J Appl Physiol
, vol.56
, Issue.4
, pp. 868-877
-
-
Knowles, M.1
Murray, G.2
Shallal, J.3
Askin, F.4
Ranga, V.5
Gatzy, J.6
Boucher, R.7
-
44
-
-
84877844941
-
Rectal forceps biopsy procedure in cystic fibrosis: technical aspects and patients perspective for clinical trials feasibility
-
3679995, 23688510
-
Servidoni MF, Sousa M, Vinagre AM, Cardoso SR, Ribeiro MA, Meirelles LR, de Carvalho RB, Kunzelmann K, Ribeiro AF, Ribeiro JD, Amaral MD. Rectal forceps biopsy procedure in cystic fibrosis: technical aspects and patients perspective for clinical trials feasibility. BMC Gastroenterol 2013, 13(1):91. 10.1186/1471-230X-13-91, 3679995, 23688510.
-
(2013)
BMC Gastroenterol
, vol.13
, Issue.1
, pp. 91
-
-
Servidoni, M.F.1
Sousa, M.2
Vinagre, A.M.3
Cardoso, S.R.4
Ribeiro, M.A.5
Meirelles, L.R.6
de Carvalho, R.B.7
Kunzelmann, K.8
Ribeiro, A.F.9
Ribeiro, J.D.10
Amaral, M.D.11
|